Abstract
Abstract. Cobalt is the scarcest of metallic micronutrients and displays a complex biogeochemical cycle. This study examines the distribution, chemical speciation, and biogeochemistry of dissolved cobalt during the US North Atlantic GEOTRACES transect expeditions (GA03/3_e), which took place in the fall of 2010 and 2011. Two major subsurface sources of cobalt to the North Atlantic were identified. The more prominent of the two was a large plume of cobalt emanating from the African coast off the eastern tropical North Atlantic coincident with the oxygen minimum zone (OMZ) likely due to reductive dissolution, biouptake and remineralization, and aeolian dust deposition. The occurrence of this plume in an OMZ with oxygen above suboxic levels implies a high threshold for persistence of dissolved cobalt plumes. The other major subsurface source came from Upper Labrador Seawater, which may carry high cobalt concentrations due to the interaction of this water mass with resuspended sediment at the western margin or from transport further upstream. Minor sources of cobalt came from dust, coastal surface waters and hydrothermal systems along the Mid-Atlantic Ridge. The full depth section of cobalt chemical speciation revealed near-complete complexation in surface waters, even within regions of high dust deposition. However, labile cobalt observed below the euphotic zone demonstrated that strong cobalt-binding ligands were not present in excess of the total cobalt concentration there, implying that mesopelagic labile cobalt was sourced from the remineralization of sinking organic matter. In the upper water column, correlations were observed between total cobalt and phosphate, and between labile cobalt and phosphate, demonstrating a strong biological influence on cobalt cycling. Along the western margin off the North American coast, this correlation with phosphate was no longer observed and instead a relationship between cobalt and salinity was observed, reflecting the importance of coastal input processes on cobalt distributions. In deep waters, both total and labile cobalt concentrations were lower than in intermediate depth waters, demonstrating that scavenging may remove labile cobalt from the water column. Total and labile cobalt distributions were also compared to a previously published South Atlantic GEOTRACES-compliant zonal transect (CoFeMUG, GAc01) to discern regional biogeochemical differences. Together, these Atlantic sectional studies highlight the dynamic ecological stoichiometry of total and labile cobalt. As increasing anthropogenic use and subsequent release of cobalt poses the potential to overpower natural cobalt signals in the oceans, it is more important than ever to establish a baseline understanding of cobalt distributions in the ocean.
Highlights
Cobalt is the scarcest of biologically utilized metals and has a complex marine biogeochemical cycle
The dissolved cobalt data product from USGT10 and USGT11 consisted of 11 and 21 profiles, respectively, totaling 717 total dissolved cobalt and 717 labile cobalt data points that were compiled into ocean sections that were rendered with Ocean Data View (Figs. 2a–b, 3; Schlitzer, 2011)
In mesopelagic waters, differences were observed within a water mass characterized as > 55 % Upper Circumpolar Deepwater (UCPDW) via optimum multi-parameter analysis (OMPA; Jenkins et al, 2015), indicating some temporal variability at these depths even within the relatively short timescale between samplings
Summary
Cobalt is the scarcest of biologically utilized metals and has a complex marine biogeochemical cycle. Noble et al.: Coastal sources, sinks and strong organic complexation of dissolved cobalt imum zones (OMZs) of the South Atlantic and South Pacific (Hawco et al, 2016; Noble et al, 2012), and from more limited datasets from the North Pacific (Ahlgren et al, 2014; Saito et al, 2004, 2005), are likely due to reductive dissolution and advection of sedimentary sources in regions with low-oxygen bottom water sediment–water interfaces (Heggie and Lewis, 1984). While cobalt has been found to be enriched in end-member hydrothermal fluids up to 2570 nM at TAG in the North Atlantic Mid-Atlantic Ridge (Metz and Trefrey, 2000), input is thought to be relatively localized to near-vent environments due to rapid removal by precipitating manganese and iron oxyhydroxides
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